The STEMRI trial: Magnetic resonance spectroscopy imaging can define tumor areas enriched in glioblastoma stem-like cells

Author:

Lemarié Anthony12ORCID,Lubrano Vincent34,Delmas Caroline15ORCID,Lusque Amélie6ORCID,Cerapio Juan-Pablo1ORCID,Perrier Marion1,Siegfried Aurore17,Arnauduc Florent12ORCID,Nicaise Yvan12ORCID,Dahan Perrine1,Filleron Thomas6,Mounier Muriel8,Toulas Christine19ORCID,Cohen-Jonathan Moyal Elizabeth1210ORCID

Affiliation:

1. CRCT, Université de Toulouse, Inserm, CNRS, Université Toulouse III–Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.

2. UFR Santé, Université de Toulouse III–Paul Sabatier, Toulouse, France.

3. TONIC, Université de Toulouse, Inserm, CNRS, Université Toulouse III–Paul Sabatier, Toulouse Neuro Imaging Center, Toulouse, France.

4. CHU de Toulouse, Neurosurgery Department, Toulouse, France.

5. Institut Claudius Regaud, IUCT-Oncopole, Interface Department, Toulouse, France.

6. Institut Claudius Regaud, IUCT-Oncopole, Biostatistics and Health Data Science Unit, Toulouse, France.

7. CHU de Toulouse, Anatomopathology Department, Toulouse, France.

8. Institut Claudius Regaud, IUCT-Oncopole, Clinical Trials Office, Toulouse, France.

9. Institut Claudius Regaud, IUCT-Oncopole, Cancer Biology Department, Molecular Oncology Division, Toulouse, France.

10. Institut Claudius Regaud, IUCT-Oncopole, Radiation Oncology Department, Toulouse, France.

Abstract

Despite maximally safe resection of the magnetic resonance imaging (MRI)–defined contrast-enhanced (CE) central tumor area and chemoradiotherapy, most patients with glioblastoma (GBM) relapse within a year in peritumoral FLAIR regions. Magnetic resonance spectroscopy imaging (MRSI) can discriminate metabolic tumor areas with higher recurrence potential as CNI+ regions (choline/ N -acetyl-aspartate index >2) can predict relapse sites. As relapses are mainly imputed to glioblastoma stem-like cells (GSCs), CNI+ areas might be GSC enriched. In this prospective trial, 16 patients with GBM underwent MRSI/MRI before surgery/chemoradiotherapy to investigate GSC content in CNI−/+ biopsies from CE/FLAIR. Biopsy and derived-GSC characterization revealed a FLAIR/CNI+ sample enrichment in GSC and in gene signatures related to stemness, DNA repair, adhesion/migration, and mitochondrial bioenergetics. FLAIR/CNI+ samples generate GSC-enriched neurospheres faster than FLAIR/CNI−. Parameters assessing biopsy GSC content and time-to-neurosphere formation in FLAIR/CNI+ were associated with worse patient outcome. Preoperative MRI/MRSI would certainly allow better resection and targeting of FLAIR/CNI+ areas, as their GSC enrichment can predict worse outcomes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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